Canonical Allele Identifier: CA395954667

Gene: GNAO1

Linked Data

• MyVariant Identifiers: chr16:g.56385335T>A (hg19) ; chr16:g.56351423T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56351423T>A , CM000678.2:g.56351423T>A	GRCh38
NC_000016.9:g.56385335T>A , CM000678.1:g.56385335T>A	GRCh37
NC_000016.8:g.54942836T>A	NCBI36
NG_042800.1:g.165085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262493.12:c.763T>A MANE Select	ENSP00000262493.6:p.Cys255Ser
ENST00000562316.6:c.430T>A	ENSP00000457238.2:p.Cys144Ser
ENST00000564727.2:c.67T>A	ENSP00000454971.2:p.Cys23Ser
ENST00000568375.2:c.116-3443T>A
ENST00000638185.1:n.978T>A
ENST00000638210.1:n.1063T>A
ENST00000638705.1:c.763T>A	ENSP00000491223.1:p.Cys255Ser
ENST00000638836.1:n.673T>A
ENST00000639055.1:n.1484T>A
ENST00000639251.1:n.664T>A
ENST00000639268.1:c.398T>A
ENST00000639341.1:c.288T>A
ENST00000639770.1:c.801T>A	ENSP00000491999.1:n.801T>A
ENST00000640390.1:n.693T>A
ENST00000640469.1:c.127T>A	ENSP00000491875.1:p.Cys43Ser
ENST00000640560.1:n.539T>A
ENST00000640893.1:c.*161T>A	ENSP00000492677.1:n.*161T>A
ENST00000262493.10:c.763T>A	ENSP00000262493.6:p.Cys255Ser
ENST00000568375.1:n.116-3443T>A
NM_020988.2:c.763T>A	NP_066268.1:p.Cys255Ser
XM_011523003.1:c.637T>A	XP_011521305.1:p.Cys213Ser
XM_011523003.3:c.637T>A	XP_011521305.1:p.Cys213Ser
NM_020988.3:c.763T>A MANE Select	NP_066268.1:p.Cys255Ser